ENST00000601549.2:n.454A>T
|
|
|
ENST00000648053.1:n.264A>T
|
|
|
ENST00000648319.1:c.832A>T
MANE Select
|
ENSP00000496939.1:p.Thr278Ser
|
|
ENST00000262888.7:c.832A>T
|
ENSP00000262888.3:p.Thr278Ser
|
|
ENST00000598836.1:c.11A>T
|
|
|
ENST00000599720.5:c.*102A>T
|
ENSP00000472513.1:n.*102A>T
|
|
ENST00000600408.1:c.121A>T
|
ENSP00000472510.1:p.Thr41Ser
|
|
ENST00000601549.1:n.141A>T
|
|
|
ENST00000615047.4:c.436A>T
|
ENSP00000485014.1:p.Thr146Ser
|
|
NM_002250.2:c.832A>T
|
NP_002241.1:p.Thr278Ser
|
|
XM_005258882.2:c.736A>T
|
XP_005258939.1:p.Thr246Ser
|
|
XM_005258883.2:c.643A>T
|
XP_005258940.1:p.Thr215Ser
|
|
XR_935823.1:n.2078A>T
|
|
|
XR_002958313.1:n.2224A>T
|
|
|
NM_002250.3:c.832A>T
MANE Select
|
NP_002241.1:p.Thr278Ser
|
|